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Lactate released by inflammatory bone marrow neutrophils induces their mobilization via endothelial GPR81 signaling

Nature communications, 2020-07, Vol.11 (1), p.3547-3547, Article 3547

2020

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PDCD10 gene mutations in multiple cerebral cavernous malformations

PloS one, 2014-10, Vol.9 (10), p.e110438-e110438

2014

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Enhanced thrombin/PAR1 activity promotes G-CSF- and AMD3100-induced mobilization of hematopoietic stem and progenitor cells via NO upregulation

Leukemia, 2021-11, Vol.35 (11), p.3334-3338

2021

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Lack of relationship between the P413L chromogranin B variant and a SALS Italian cohort

Gene, 2015-09, Vol.568 (2), p.186-189

2015

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Role of fructosamine-3-kinase in protecting against the onset of microvascular and macrovascular complications in patients with T2DM

BMJ open diabetes research & care, 2020-05, Vol.8 (1), p.e001256

2020

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PAR1 Expression Predicts Clinical G‐CSF CD34+ HSPC Mobilization and Repopulation Potential in Transplanted Patients

HemaSphere, 2019-10, Vol.3 (5), p.1-4

2019

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VLA-4 Affinity Assay for Murine Bone Marrow-derived Hematopoietic Stem Cells

Bio-protocol, 2017-02, Vol.7 (4), p.e2134-e2134

2017

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Adhesion Assay for Murine Bone Marrow Hematopoietic Stem Cells

Bio-protocol, 2017-02, Vol.7 (4), p.e2135-e2135

2017

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Reactivation of Fetal Hemoglobin in Thalassemia and Sickle Cell Disease

Thalassemia reports, 2014-01, Vol.4 (2), p.2196

2014

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Wide phenotypic spectrum of the TARDBP gene: homozygosity of A382T mutation in a patient presenting with amyotrophic lateral sclerosis, Parkinson's disease, and frontotemporal lobar degeneration, and in neurologically healthy subject

Neurobiology of aging, 2012-08, Vol.33 (8), p.1846.e1-1846.e4

2012

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Nocturnal Melatonin Renews Bone and Blood Forming Stem Cells Reservoir By Metabolic Reprograming

Blood, 2018-11, Vol.132 (Supplement 1), p.3326-3326

2018

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Acute Inflammation Induces Lactate Release By Bone Marrow Neutrophils That Promotes Their Mobilization Via Endothelial GPR81 Signaling

Blood, 2019-11, Vol.134 (Supplement_1), p.3582-3582

2019

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Possible role of fructosamine 3-kinase genotyping for the management of diabetic patients

Clinical chemistry and laboratory medicine, 2015-08, Vol.53 (9), p.1315

2015

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Corrigendum to “Lack of relationship between the P413L chromogranin B variant and a SALS Italian cohort” [GENE 568/2 (2015) 186–189]

Gene, 2016-04, Vol.581 (1), p.94-94

2016

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Lactate Release By Bone Marrow Neutrophils Promotes Their Inflammatory Mobilization Via Endothelial GPR81 Signaling

Blood, 2017-12, Vol.130, p.446-446

2017

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Inverse PAR1 Activity of Hematopoietic Stem Cells and BM Stromal Cells Mediates G-CSF-Induced Mobilization By Regulation of Nitric Oxide Generation

Blood, 2016-12, Vol.128 (22), p.3370-3370

2016

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EPCR Guides Hematopoietic Stem Cells Homing to the Bone Marrow Independently of Niche Clearance

Blood, 2016-12, Vol.128 (22), p.4538-4538

2016

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Reactivation of fetal hemoglobin in thalassemia and sickle cell disease

Thalassemia reports, 2014-09, Vol.4 (1s)

2014

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Phenotypic Heterogeneity in a SOD1 G93D Italian ALS Family: An Example of Human Model to Study a Complex Disease

Journal of molecular neuroscience, 2011-05, Vol.44 (1), p.25-30

2011

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De Novo MGC4607 Gene Heterozygous Missense Variants in a Child with Multiple Cerebral Cavernous Malformations

Journal of molecular neuroscience, 2012-07, Vol.47 (3), p.475-480

2012

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PDCD10 Gene Mutations in Multiple Cerebral Cavernous Malformations: e110438

PloS one, 2014-10, Vol.9 (10)

2014

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Mutation in the senataxin gene found in a patient affected by familial ALS with juvenile onset and slow progression

Amyotrophic lateral sclerosis, 2011-05, Vol.12 (3), p.228-230

2011

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Lactate released by inflammatory bone marrow neutrophils induces their mobilization via endothelial GPR81 signaling

PDCD10 gene mutations in multiple cerebral cavernous malformations

Daily Onset of Light and Darkness Differentially Controls Hematopoietic Stem Cell Differentiation and Maintenance

Enhanced thrombin/PAR1 activity promotes G-CSF- and AMD3100-induced mobilization of hematopoietic stem and progenitor cells via NO upregulation

Lack of relationship between the P413L chromogranin B variant and a SALS Italian cohort

Role of fructosamine-3-kinase in protecting against the onset of microvascular and macrovascular complications in patients with T2DM

PAR1 Expression Predicts Clinical G‐CSF CD34+ HSPC Mobilization and Repopulation Potential in Transplanted Patients

VLA-4 Affinity Assay for Murine Bone Marrow-derived Hematopoietic Stem Cells

Adhesion Assay for Murine Bone Marrow Hematopoietic Stem Cells

Reactivation of Fetal Hemoglobin in Thalassemia and Sickle Cell Disease

Wide phenotypic spectrum of the TARDBP gene: homozygosity of A382T mutation in a patient presenting with amyotrophic lateral sclerosis, Parkinson's disease, and frontotemporal lobar degeneration, and in neurologically healthy subject

Nocturnal Melatonin Renews Bone and Blood Forming Stem Cells Reservoir By Metabolic Reprograming

Acute Inflammation Induces Lactate Release By Bone Marrow Neutrophils That Promotes Their Mobilization Via Endothelial GPR81 Signaling

Possible role of fructosamine 3-kinase genotyping for the management of diabetic patients

Corrigendum to “Lack of relationship between the P413L chromogranin B variant and a SALS Italian cohort” [GENE 568/2 (2015) 186–189]

Lactate Release By Bone Marrow Neutrophils Promotes Their Inflammatory Mobilization Via Endothelial GPR81 Signaling

Inverse PAR1 Activity of Hematopoietic Stem Cells and BM Stromal Cells Mediates G-CSF-Induced Mobilization By Regulation of Nitric Oxide Generation

EPCR Guides Hematopoietic Stem Cells Homing to the Bone Marrow Independently of Niche Clearance

Reactivation of fetal hemoglobin in thalassemia and sickle cell disease

Phenotypic Heterogeneity in a SOD1 G93D Italian ALS Family: An Example of Human Model to Study a Complex Disease

De Novo MGC4607 Gene Heterozygous Missense Variants in a Child with Multiple Cerebral Cavernous Malformations

PDCD10 Gene Mutations in Multiple Cerebral Cavernous Malformations: e110438

Mutation in the senataxin gene found in a patient affected by familial ALS with juvenile onset and slow progression

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